Abstract: A minimally invasive circulatory support platform that utilizes an aortic stent pump or pumps. The platform uses a low profile catheter-based techniques and provides temporary and chronic circulatory support depending on the needs of the patient. Also described is a catheter-based temporary assist pump to treat patients with acute decompensated heart failure and provide circulatory support to subjects undergoing high risk percutaneous coronary intervention (“PCI”). Further described is a wirelessly powered circulatory assist pump for providing chronic circulatory support for heart failure patients. The platform and system are relatively easy to place, have higher flow rates than existing systems, and provide improvements in the patient's renal function.

Abstract: The glove application device enables the placement of a glove on a glove retainer. An inverted glove is provided to the user to simplify placement of the glove on the glove retainer. The inverted glove presents a donning surface for insertion of the user's hands when installed onto the glove retainer. A glove indicator on the glove aligns with an orientation indicator, such as a particular location on the glove retainer, a component, or a device indicator. The application device provides an indicator such as a release toggle, a device indicator, or other component of the device that informs the user of the proper orientation of the glove when placing the glove on the glove retainer.

Abstract: The glove dispensing device enables the placement of a glove on a glove retainer. The placement of the glove on the glove retainer at least partially seals the glove with the glove retainer. The user activates a vacuum that draws the glove into a housing of the glove dispensing device. The vacuum inverts the glove thus opening the glove to allow placement of the user's hand within the glove. The user may then remove his hand with the glove from the glove retainer. To assist with removing the glove from the glove retainer, the glove dispensing device provides a release toggle stored within the glove retainer. The user adjusts the release toggle to break the seal of the glove with the glove retainer. Breaking the seal overcomes the pressure applied to the glove from the vacuum. Thus, the glove is applied to the user's hand and ready for use.

Abstract: The glove dispensing device enables the placement of a glove on a glove retainer. The placement of the glove on the glove retainer at least partially seals the glove with the glove retainer. The user activates a vacuum that draws the glove into a housing of the glove dispensing device. The vacuum inverts the glove thus opening the glove to allow placement of the user's hand within the glove. The user may then remove his hand with the glove from the glove retainer. To assist with removing the glove from the glove retainer, the glove dispensing device provides a release toggle stored within the glove retainer. The user adjusts the release toggle to break the seal of the glove with the glove retainer. Breaking the seal overcomes the pressure applied to the glove from the vacuum. Thus, the glove is applied to the user's hand and ready for use.

Abstract: A cannula for a patient includes an elongate body having a length of at least 70 cm and a channel extending through the body defining a wall. The cannula includes a wire embodied within at least a portion of the wall. The body has a proximal end, a distal end having a tip opening through which the channel extends and a plurality of side holes through the wall in proximity to the tip for unimpeded flow of blood at the distal end. The cannula includes a barbed fitting at the proximal end. The cannula includes a suture wing for securing the elongated body to the patient. A system for assisting a patient's heart. A method for assisting a patient's heart.

Abstract: Systems and methods for automated estate management. Estate data for an estate is received. Allowable entities authorized to access the estate data are determined. Portions of the estate data that the entities are allowed to access are determined. At least one access condition that needs to be met in order to allow the entities to access the portions of the estate data are determined. Whether the at least one access condition is met is determined. Access is provided for the entities to the portions of the estate data that the entities are authorized to access if it is determined that the at least one access condition is met.

Abstract: Systems and methods for managing accounts associated with an estate. Estate data for an estate is received. The received estate data is verified. Closing data is generated for an account associated with the estate using the estate data. The closing data for the account is used to facilitate closing the account associated with the estate. In facilitating closing of the account associated with the estate, the closing data is sent to a first account system for the account to cause the account to be closed.

Abstract: A system comprises a processor; a communications engine for receiving a request to determine potential service provider accounts that a user has with one or more service providers and for obtaining financial data records of the user from an API that obtains the financial data records from a financial provider system, each respective financial data record corresponding to a respective transaction and including a respective date, amount, and party identifier corresponding to a respective party associated with the respective transaction; a confidence score determination engine for evaluating the financial data records to generate a particular confidence score corresponding to a particular party, the particular confidence score indicating a likelihood that the user has a service provider account with the particular party; and a potential service provider account identification engine for identifying the potential service provider account based on the particular confidence score.

Abstract: An extracorporeal blood cooling or heating circuit includes an intravenous catheter for withdrawing a patients blood coupled to a combined pump/heat exchanger device. One or more sensors are provided upstream and/or downstream of the pump/heat exchanger device for measuring pressure, temperature, fluid flow, blood oxygenation, and other parameters. A controller is operatively coupled to the pump/heat exchanger device and the one or more sensors to control the speed of the pump inside the pump/heat exchanger device and regulate the blood temperature by controlling the operation of the heat exchanger. The combined pump/heat exchanger device includes a housing having at least one inlet and at least one outlet, a pump portion defining a blood circuit inside the housing, and a heat exchanger portion contained within the housing for selectively heating or cooling the blood.

Abstract: A cannula for a patient includes an elongate body having a length of at least 70 cm and a channel extending through the body defining a wall. The cannula includes a wire embodied within at least a portion of the wall. The body has a proximal end, a distal end having a tip opening through which the channel extends and a plurality of side holes through the wall in proximity to the tip for unimpeded flow of blood at the distal end. The cannula includes a barbed fitting at the proximal end. The cannula includes a suture wing for securing the elongated body to the patient. A system for assisting a patient's heart. A method for assisting a patient's heart.

Abstract: A system for assisting the right heart of a patient includes a PA cannula adapted for insertion into a PA of a patient through the right internal jugular vein of the patient. The system includes a percutaneous RA cannula adapted for insertion into an RA of the patient. The system includes a blood pump disposed outside of the patient to which the RA cannula and the PA cannula are connected to provide right ventricular circulatory support to the patient without any left ventricular assist. A method for assisting the right heart of a patient includes the steps of inserting a PA cannula into a PA of a patient. There is the step of inserting an RA cannula into an RA of the patient. There is the step of connecting the RA cannula and the PA cannula to a blood pump disposed outside of the patient. There is the step of activating the blood pump to provide right ventricular circulatory support to assist the heart of the patient.

Abstract: The invention is apparatus for communicating between a subscriber and a second party in a 2-way texting system. The apparatus includes a hosted application system, having a host application server, storage, communication apparatus and a hosted application. A subscriber's 2-way communication device is coupled to the communication apparatus and assigned a unique designator. The hosted application system is coupled to receive a message and designated recipient from a message originator's 2-way communication device. The message originator is one of the subscriber and the second party, and the recipient is the other of the subscriber and the second party. The hosted application converts the message to a designated format and delivers the message using the unique designator, to the recipient's 2-way communication device. The message can be responded to by the recipient using the unique designator.

Abstract: An MIE apparatus has a blower, a direction valve, an oscillator, and a mask hose connector. The blower is connected to the direction valve, which is connected to the oscillator, which is connected to the hose connector. During insufflation, a direction valve connects exhaust of a blower to an oscillator, causing positive pressure at the hose connector. During exsufflation, the direction valve connects the blower intake to the oscillator, causing negative pressure at the hose connector. The oscillator is a butterfly valve with a 360° rotating disc. During insufflation, the disc is fixed to steadily modulate the airflow. During exsufflation, the oscillator is inactive or in flutter mode. When inactive, the disc is fixed to allow maximum air flow. In flutter mode, the disc continuously rotates so that the air flow rapidly alternates between maximum and minimum.

Abstract: An apparatus for treating a patient. The apparatus includes a catheter having a distal end and a proximal end. The distal end has an orifice through which a fluid can flow. The distal end has a port through which the fluid can flow. The port is adjacent to but apart from the orifice. The apparatus includes a mechanism for controlling the size of the port that is open. The controlling mechanism is disposed over the port and able to close the port. An apparatus for treating a patient. The apparatus includes a catheter having a proximal end and a distal end having an orifice through which a fluid can flow. The distal end has an end marker disposed about the orifice which appears in an image of an imaging device. An apparatus for treating a patient. The apparatus includes a catheter having a proximal end and a distal end having an orifice through which fluid can flow. The catheter has an axis.

Abstract: A bottle cap remover includes a pair of axially nested socket sections of different diameters depending axially from a larger-diameter grasping section. Each of the socket sections includes frictional gripping members along their inner walls that are adapted to frictionally engage different sizes and types of metal and plastic bottle caps, thereby to enable the user to twist off and remove the bottle caps by applying a relatively small twisting force to the grasping section.

Abstract: The invention includes an improved handpiece for use in a microdermabrasion system. The handpiece includes a control line which allows the user to easily control activation of the compressor, a vacuum line and a compressor line. The microdermabrasion system includes a vacuum pump, compressor, and a mixing bottle. A pressure sensor is used to detect pressure changes in the system for use in activating/deactivating the compressor.

Abstract: An apparatus for treating a patient. The apparatus includes a catheter having a distal end and a proximal end. The distal end has an orifice through which a fluid can flow. The distal end has a port through which the fluid can flow. The port is adjacent to but apart from the orifice. The apparatus includes a mechanism for controlling the size of the port that is open. The controlling mechanism is disposed over the port and able to close the port. An apparatus for treating a patient. The apparatus includes a catheter having a proximal end and a distal end having an orifice through which a fluid can flow. The distal end has an end marker disposed about the orifice which appears in an image of an imaging device. An apparatus for treating a patient. The apparatus includes a catheter having a proximal end and a distal end having an orifice through which fluid can flow. The catheter has an axis.

Abstract: A system of head rests is disclosed for use by patients convalescing from optical surgery to re-attach a detached retina. In this procedure, a bubble of air is injected into the affected eye, and the patient is instructed to keep his or her head in a face-downward position for eighteen hours a day during a convalescent period in which the air bubble presses the retina against the back wall of the eyeball. A day-time version of the apparatus is adjustable in height and preferably incorporates armrests and a plurality of mirrors so that a person who has his face turned toward the floor may view television or may make eye contact with another person. A night-time version of the apparatus allows a person to lie in a prone position with his or her head supported above and out of contact with the mattress, and preferably includes a viewing window so that a prone patient can read a book placed on the floor.

Abstract: An alarm system providing external alarm signals for a structure. The alarm system includes transmitters for generating coded radio trigger signals. An alarm controller located in the interior of the structure is responsive to the coded radio trigger signals for generating alarm actuation signals. The alarm actuation signals are transmitted to alarm signal generators located on the exterior of the structure. Transmission lines for the alarm actuation signals are connected between the alarm controller and the alarm signals generators. Integrity determination of the transmission lines is provided by detection of a break in a current loop provided by a ground line and a ground sense line connected between the controller and the alarm signal generators along side the transmission lines.